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Completed

NCT Number: NCT06579430

Diagnostic Accuracy Study of Indocyanine Green for Perfusion Assessment

Background Near-infrared fluorescence guided surgery with indocyanine green (ICG) was introduced for parathyroid perfusion assessment during total thyroidectomy in 2016. ICG can visualize tissue perfusion, since it becomes completely and permanently fixed to plasma proteins in the bloodstream, and circulates in the intravascular compartment only. ICG was already approved in 1956 for clinical use of tissue perfusion. However, until now there is still no (parathyroid) universal standard imaging protocol for ICG-guided fluorescent surgery including quantitative evaluation.

Main research question To develop a standardized universal imaging protocol for the assessment of parathyroid perfusion during total thyroidectomy with ICG including quantitative evaluation of the fluorescent signal.

• Design (including population, confounders/outcomes) This will be a proof-of-concept, prospective cohort study of patients undergoing an ICG-guided fluorescent total thyroidectomy to evaluate parathyroid gland perfusion. The main study endpoint is quantification of the fluorescent signal of ICG stratified by the occurrence of hypoparathyroidism. Hypoparathyroidism will be defined as a decrease in PTH of >70% at the first postoperative day. Furthermore, we will calculate the sensitivity of our model for the prediction of hypoparathyroidism.

Secondary outcomes are data from surgery, pre- and postoperative lab values (including calcium, PTH, albumin) and postoperative medication use.

Expected results We expect that the results of this study will lead to the development of a universal standard imaging protocol for ICG-guided fluorescent total thyroidectomy.

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Key information

Age range

18 year and older

Sex eligibility

All sexes

Study type

Interventional

Phase

Early Phase 1

Primary location

University Medical Center Groningen, Groningen, Netherlands

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Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • Age >18 years
  • Patients undergoing ICG-guided total thyroidectomy as surgical procedure for thyroid cancer, Graves' disease or goiter
  • Patients are eligible for surgery
  • Patients are mentally competent
  • Written informed consent

Exclusion criteria

  • Patients with known allergy for ICG or iodinated contrast
  • Pregnant or lactating women
  • Patients with previous neck surgery
  • Patients with dialysis dependent renal failure and kidney transplant

Treatment and study plan

Indocyanine Green near infrared fluorescence imaging

Drug

ICG-NIRF was performed using the Quest Spectrum Platform 2.0. The camera lens was positioned at a fixed distance of 30 cm to the wound bed, at a perpendicular angle, with the gain set at 22.5 decibels (dB) and an exposure time of 50 milliseconds (ms). ICG was dissolved in sterile water at a concentration of 2.5 mg/mL as recommended by the manufacturer (Verdye). 1.5 mg of ICG per liter of circulating blood volume was then administered through manual bolus intravenous injection. Blood volume estimation was based on the patient's height and weight.

Other names: Multicenter cohort

Primary outcomes

  1. Injection speed

    Time frame: During surgery

    The impact of injection speed on a parathyroid perfusion curve (slow vs fast)

  2. ICG concentration

    Time frame: During surgery

    The impact of ICG concentration on a parathyroid perfusion curve (2.5 mg/mL vs 0.5 mg/mL)

  3. Camera system

    Time frame: During surgery

    The impact of a camera system on a parathyroid perfusion curve (Quest vs SpyElite)

Secondary outcomes

  1. Multicenter application

    Time frame: From surgery until one day post-surgery

    The correlation between postoperative hypoparathyroidism and the perfusion curve in two different centers (UMCG/EMC)

Sponsors and collaborators

Lead sponsor

University Medical Center Groningen

Other

Collaborators

  • Erasmus Medical Center
  • Leiden University Medical Center

Registry information

Acronym: Pre-CLOVER

Important dates

Study start
2020
Primary completion
2024
Study completion
2024
First posted
Aug 30, 2024
Registry last updated
Sep 19, 2024

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

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This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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